Ivenix Infusion System (IIS), Large Volume Pump LVP-0004
FDA Recall Z-0549-2024 · Posted 2023-12-20
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Recalling FirmFresenius Kabi USA, LLC
Recall StatusOpen, Classified
Product CodeFRN
Date Initiated2023-11-29
Product Quantity938 US
Reason for Recall
The device may experience mechanical interference on the Fluid Valve pins, which will trigger a Pump Problem alarm. The issue may lead to delay or interruption of therapy. Depending on the therapy and duration of delay/interruption, the issue may lead to serious harm or death.
Firm Action
On November 29, 2023, the firm began notifying affected customers via" URGENT-Medical Device Recall" letter dated November 28, 2023.
Customers were provided with precautions to take until the affected LVPs are able to be returned for repair or replacement of internal hardware.
Customers will be contacted by a Fresenius Kabi service representative to create a plan for addressing any affected LVPs at their facility. This effort is expected to begin in January 2024. Fresenius Kabi will repair LVPs that may encounter mechanical interference causing the Fluid Valve Actuation System not to move properly. If the LVP cannot be repaired, it will be replaced at no cost to the customer.
If you have any questions contact Customer support at, email: [email protected] or phone at 1-978-775-8100.
Root Cause
Process change control
Distribution Pattern
US distribution to states of: CA, CO, NJ, UT, and WI.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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